Find research datasets worth reusing

Fig. 8 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 8. Habitus of Anthocoris spp., male, dorsal (A, C–E, G–H) and lateral (B, F) views. A–B – A. miyamotoi Hiura, 1959, holotype (Nakanoshima Is., Tokara Isls.); C – same (Wakayama, Honshu); D – same (Kagoshima, Kyushu); E–F – A. venustus sp. nov., holotype (Hokkaido); G – same, paratype (Tochigi, Honshu); H – same, paratype (Nara, Honshu). Scale bars: 1.0 mm.

Fig. 4 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 4. Habitus, dorsal (A, C, E, G) and lateral (B, D, F, H) views. A–B – Acompocoris brevirostris Kerzhner, 1979, male; C–D – same, female; E–F – Tetraphleps aterrima (J. Sahlberg, 1878), male; G–H – same, female. Scale bars: 1.0 mm.

Fig. 13 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 13. Male genitalia of Anthocoris spp. A–C – A. chibi Hiura, 1959; D–F – A. confusus Reuter, 1884; G–I – A. japonicus Poppius, 1909; J–L – A. nemoralis (Fabricius, 1794); M–O – A. takahashii Hiura, 1959. A, D, G, J, M – pygophore with paramere (ejaculatory bulb omitted), dorsal view; B–C, E–F, H–I, K–L, N–O – paramere, two different views. Abbreviations: prm ‒ paramere; pyg ‒ pygophore. Scale bars: 0.1 mm.

Fig. 15 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 15. Female genitalia of Anthocoris spp., dorsal view.A – A. chibi Hiura, 1959; B – A. confusus Reuter, 1884; C – A. japonicus Poppius, 1909; D – A. nemoralis (Fabricius, 1794); E – A. takahashii Hiura, 1959; F – A. miyamotoi Hiura, 1959; G – A. venustus sp. nov., paratype.Abbreviations: ct ‒ copulatory tube; ism ‒ intersegmental membrane; sp ‒ sperm pouch; t ‒ trunk of conductive tissue (C–D, trunk of conductive tissue dissolved). Scale bars: 0.1 mm.

Fig. 5 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 5. Scanning electron micrographs of diagnostic characters of Japanese anthocorids. A–C – Acompocoris brevirostris Kerzhner, 1979, female (A) and male (B–C); D–F – Tetraphleps aterrima (J. Sahlberg, 1878), male. A, D – ostiolar peritreme and evaporatorium, left lateroventral view; B, E – pygophore with paramere, dorsal view; C, F – paramere, dorsal views. Abbreviations: eva ‒ evaporatorium; mf ‒ median furrow; op ‒ ostiolar peritreme; prm ‒ paramere; pyg ‒ pygophore.

Fig. 1 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 1. Habitus, dorsal (A, C, E) and lateral (B, D, F) views. A–B – Temnostethus distans Kerzhner, 1973, female; C–D – T. mirificus sp. nov., holotype, male; E–F – Elatophilus nipponensis Hiura, 1966, male. Scale bars: 1.0 mm.

Model output, Khaled et al., Iron distribution in the aqueous phase (short title)

Data for figures (Khaled et al., The number fraction of iron-containing particles affects OH, HO2 and H2O2 budgets in the atmospheric aqueous phase, Atmos. Chem. Phys.)

opencc-zeroJan 2022View details →

dryad40/100

Using species distribution models and decision tools to direct surveys and identify potential translocation sites for a critically endangered species

Aim: Occurrence records for cryptic species are typically limited or highly uncertain, leaving their distributions poorly resolved and hampering conservation. This can apply to well‐studied species, and increased survey effort and/or novel methods are required to improve distribution data. Here, we paired species distribution modelling (SDM) with decision tools to direct surveys for the critically endangered Leadbeater's possum (Gymnobelideus leadbeateri) outside its current restricted range. We also assessed survey areas for their suitability to host translocations. Location: Victoria, Australia. Method: We used both recent and historic records (now out of range and spatially uncertain) of Leadbeater's possum to build SDMs using MaxEnt. The SDMs informed an initial multi‐criteria decision analysis (MCDA) that enabled prioritization of 80 survey sites across seven forest patches (13–145 km outside the known range), which we surveyed using camera traps. Site and vegetation data were used in a post‐survey MCDA to rank their potential translocation suitability. Results: The SDM predictions were consistent with the species' ecology, identifying cold areas with high rainfall that had not recently burnt as suitable. The spatial uncertainty of records did not exert a strong influence on either model predictions or the ranking of patches for surveys. Camera trap surveys yielded records of 19 native species, with Leadbeater's possum detected in only one survey patch, 13 km outside of its previously known range. The post‐survey MCDA identified three forest patches as potentially suitable for conservation translocations, and these priorities were not sensitive to the decision criteria used. Main conclusions: The approach outlined here prioritized survey effort over a large area, resulting in detection of Leadbeater's possum in one new patch. The potential translocation sites identified could present an important risk‐spreading measure for the species given the threat posed by bushfire. Combining SDMs and decision tools can help target surveys and guide subsequent conservation strategies.

dryad40/100

Thermal tolerance in Drosophila: repercussions for distribution, community coexistence and responses to climate change

Here we combined controlled experiments and field surveys to determine if estimates of heat tolerance predict distributional ranges and phenology of different Drosophila species in southern South America. We contrasted thermal death time curves, which consider both magnitude and duration of the challenge to estimate heat tolerance, against the thermal range where populations are viable based on field surveys in an 8-yr longitudinal study. We observed a strong correspondence of the physiological limits, the thermal niche for population growth, and the geographic ranges across studied species, which suggests that the thermal biology of different species provides a common currency to understand how species will respond to warming temperatures both at a local level and throughout their distribution range. Our approach represents a novel analytical toolbox to anticipate how natural communities of ectothermic organisms will respond to global warming.

opencc-zeroJan 2022View details →

Environment and density-dependency explain the fine-scale distribution of tree recruits before and after thinning

Dataset used in the article "Environment and density-dependency explain the fine-scale distribution of tree recruits before and after thinning" in PeerJ

opencc-by-4.0May 2012View details →

Figs. 372–377. Distribution maps. 372 in Noideattella and Tolegnaro, Two New Genera of Goblin Spiders from Madagascar, with Comments on the Gamasomorphoid and Silhouettelloid Oonopids (Araneae, Oonopidae)

Figs. 372–377. Distribution maps. 372. Noideattella amboa (circles), Noideattella assumptia (triangles). 373. Noideattella gamela (circles), Noideattella famafa (triangles). 374. Noideattella saka (circles), Noideattella mamba (triangles). 375. Noideattella lakana (circles), Noideattella farihy (triangles), Noideattella tany (squares). 376. Noideattella tsiba (circles), Noideattella fantara (triangles). 377. Tolegnaro sagani (circles), Tolegnaro kepleri (triangles).

Porosity distribution in sub-skin boundary area of the powderbed additively manufactured parts

Repository contains measurement results of the experimental investigationn of the sub-skin porosity in additively manufactured parts. Specimens were manufactured using machine manufacturer's suggested process parameters. Four different machines (EOS M400, TRUMPF TruPrint 1000, SLM 280 and DMG MORI LASERTEC 30 2nd gen.) and four different powder materials (mararging steel 1.2709, aluminum alloy AlSi10Mg, Titanium grade 5 and stainless steel 1.4404) are covered. Influences of the relative orientation of the hatch and boundary scanning tracks was investigated. Efficiency of the mitigation strategy againts sub-skin porosity issues through distance variation between hatch and boundary tracks was evaluated. Please refer to README.MD (or .PDF) for more detailed information about this dataset.

Dataset from "Merging Digital Humanities and Discourse Analysis in the Study of COVID-19 Vaccine Distribution in Norwegian Newspapers" (Sverdljuk et al. 2022)

Contains URNs (identifiers) for the newspapers used in the corpus study "Merging Digital Humanities and Discourse Analysis in the Study of COVID-19 Vaccine Distribution in Norwegian Newspapers". For each subcorpus there is an Excel file containing references to the objects used, together with basic metadata. The corpus definitions can be used in various webapps of the DH-LAB at the National Library of Norway, e.g.: <a href="https://beta.nb.no/dhlab/concordances/">https://beta.nb.no/dhlab/concordances/</a> <a href="https://beta.nb.no/dhlab/collocations/">https://beta.nb.no/dhlab/collocations/</a> See more at <a href="https://www.nb.no/dh-lab/">https://www.nb.no/dh-lab/</a>

Fig. 17 in A revision of the systematics and distribution of the damselfly genus Prodasineura Cowley, 1934 (Odonata: Zygoptera: Platycnemididae) in Vietnam with description of two new species

Fig. 17. Distribution map of Prodasineura Cowley, 1934 spp. in Vietnam (blue group species including the blackish P. autumnalis (Fraser, 1922)). (●) P. autumnalis. (●) P. coerulescens (Fraser, 1932). (●) P. doisuthepensis Hoess, 2007. (●) P. hoffmanni Kosterin, 2015.

Fig. 15. Prodasineura Cowley, 1934 in A revision of the systematics and distribution of the damselfly genus Prodasineura Cowley, 1934 (Odonata: Zygoptera: Platycnemididae) in Vietnam with description of two new species

Fig. 15. Prodasineura Cowley, 1934 spp., males, in nature. A. P. kong sp. nov. B. P. lancastrei sp. nov.

Fig. 14 in A revision of the systematics and distribution of the damselfly genus Prodasineura Cowley, 1934 (Odonata: Zygoptera: Platycnemididae) in Vietnam with description of two new species

Fig. 14. Habitus of Prodasineura Cowley, 1934 spp. A–B. P. kong sp. nov. A. ♂, holotype, ZCDTU 2019071811-ODO. B. ♀, paratype, ZCDTU 2019071817-ODO. C–D. P. lancastrei sp. nov., C. ♂, holotype, ZCDTU 2019051212-ODO. D. ♀, paratype, ZCDTU 2019051217-ODO. Scale bar = 1 cm.

Fig. 13 in A revision of the systematics and distribution of the damselfly genus Prodasineura Cowley, 1934 (Odonata: Zygoptera: Platycnemididae) in Vietnam with description of two new species

Fig. 13. Posterior pronotal lobe of prothorax of Prodasineura Cowley, 1934 spp., females, lateral and dorsal views. A–B. P. croconota Ris, 1916, ZCDTU 2017060802-ODO. C–D. P. kong sp. nov., ZCDTU 019071817-ODO. E–F. P. lancastrei sp. nov., ZCDTU 2019051217-ODO. G–H. P. verticalis Selys, 1860, ZCDTU 2018030611-ODO. Images not to scale.

Fig. 12 in A revision of the systematics and distribution of the damselfly genus Prodasineura Cowley, 1934 (Odonata: Zygoptera: Platycnemididae) in Vietnam with description of two new species

Fig. 12. Head of Prodasineura Cowley, 1934 spp., frontal view. A–B. P. kong sp. nov. A. ♂, holotype, ZCDTU 2019071811-ODO. B. ♀, paratype, ZCDTU 2019071817-ODO. C–D. P. lancastrei sp. nov. C. holotype, ZCDTU 2019051212-ODO. D. ♀, paratype, ZCDTU 2019051217-ODO. Images not to scale.

Fig. 10 in A revision of the systematics and distribution of the damselfly genus Prodasineura Cowley, 1934 (Odonata: Zygoptera: Platycnemididae) in Vietnam with description of two new species

Fig. 10. Wings base and genital ligula of Prodasineura Cowley, 1934 spp., males, holotypes A–B. P. kong sp. nov., ZCDTU 2019071811-ODO. C–D. P. lancastrei sp. nov., ZCDTU 2019051212-ODO. Images not to scale.

Fig. 9 in A revision of the systematics and distribution of the damselfly genus Prodasineura Cowley, 1934 (Odonata: Zygoptera: Platycnemididae) in Vietnam with description of two new species

Fig. 9. Structures of Prodasineura Cowley, 1934 spp., males, holotypes. A, C–D. P. kong sp. nov., ZCDTU 2019071811-ODO. B, E–F. P. lancastrei sp. nov., ZCDTU 2019051212-ODO. A–B = head and thorax, lateral view; C, E = appendages, lateral view; D, F = appendages, dorsal view. Images not to scale.